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895577-21-6

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895577-21-6 Usage

General Description

4-(1-BOC-AMINO-ETHYL)-BENZOIC ACID is a chemical compound with the molecular formula C16H21NO4. It is a derivative of benzoic acid with an added BOC (tert-butoxycarbonyl) protecting group attached to the aminoethyl moiety. 4-(1-BOC-AMINO-ETHYL)-BENZOIC ACID is commonly used as a building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. The BOC protecting group is often used to temporarily mask the amino functionality of a molecule during a chemical reaction, allowing for selective modification of other parts of the molecule without affecting the amino group. 4-(1-BOC-AMINO-ETHYL)-BENZOIC ACID is an important intermediate in the synthesis of various compounds for medical and agricultural applications.

Check Digit Verification of cas no

The CAS Registry Mumber 895577-21-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,5,5,7 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 895577-21:
(8*8)+(7*9)+(6*5)+(5*5)+(4*7)+(3*7)+(2*2)+(1*1)=236
236 % 10 = 6
So 895577-21-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H18O4/c1-9(13(17)18-14(2,3)4)10-5-7-11(8-6-10)12(15)16/h5-9H,1-4H3,(H,15,16)

895577-21-6 Well-known Company Product Price

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  • Aldrich

  • (JWP00073)  4-(1-Boc-amino-ethyl)-benzoic acid  AldrichCPR

  • 895577-21-6

  • JWP00073-1G

  • 13,864.50CNY

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895577-21-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[1-[(2-methylpropan-2-yl)oxy]-1-oxopropan-2-yl]benzoic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:895577-21-6 SDS

895577-21-6Downstream Products

895577-21-6Relevant articles and documents

Functionalized Chiral Bambusurils: Synthesis and Host-Guest Interactions with Chiral Carboxylates

?indelá?, Vladimír,?tefek, Adam,Sokolov, Jan

, p. 1307 - 1314 (2020/07/04)

Bambusurils are a class of macrocyclic anion receptors that exhibit notable anion recognition properties, able to bind various inorganic anions as well the carboxylates or sulfonates. Recently, we reported enantioselective recognition of chiral carboxylates using non-functionalized chiral bambusuril derivatives. Herein, we report the synthesis and host-guest properties of two new representatives of chiral bambusuril macrocycles bearing ester functional groups, differing by the substituents attached to their portals. Their supramolecular properties in terms of carboxylate binding were studied by means of NMR in DMSO-d6. The reported bambusurils bind selected chiral carboxylates with enantioselectivity factors up to 3.1. The results indicated that the selectivity towards different carboxylates is governed by the steric constraint of the substituents surrounding bambusuril portals. No clear trend in the binding affinities and their enantioselectivities was found.

METHODS OF CONTROLLING INSECTS

-

, (2014/03/25)

The present invention provides a method comprising applying to a crop of cotton plants, the locus thereof, or propagation material thereof, a compound of formula (I) wherein -B1-B2-B3-is -C=N-O-, -C=N-CH2-, or -

METHODS OF CONTROLLING INSECTS

-

, (2014/03/25)

The present invention provides provides a method for controlling and/or preventing insects from the genus of Plutella in useful plants, comprising applying to a crop of useful plants, the locus thereof, or propagation material thereof, a compound of formu

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